A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494623



Internal ID21152176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110661301..110667100hg38UCSC Ensembl
chr13:111313648..111319447hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007159
Samples
Known GenesCARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494623
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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